Preparation of aromatic amides from carbon monoxide, an amine and an aromatic chloride

Abstract

The present invention is directed to a process for preparing an aromatic amide. More specifically, the process involves reacting carbon monoxide, an amine and an aromatic chloride in the presence of an iodide or bromide salt, a catalyst, and a base.

Claims

1. A process for preparing an aromatic amide, said process comprising reacting:

(A) carbon monoxide;

(B) a primary or secondary amine having the structure: ##STR13## wherein x is 1, 2 or 3; R is selected from the group consisting of an alkyl group having 2 to 23 carbon atoms and an aryl group having 6 to 14 carbon atoms; and R.sup.1 is selected from the group consisting of hydrogen, an alkyl group having 1 to 20 carbon atoms and an aryl group having 5 to 14 carbon atoms; and

(C) an aromatic chloride having the following structure: ##STR14## wherein y is 1, 2, or 3; z is 1 or 2; R.sup.2 is selected from the group consisting of an alkyl group having 1 to 20 carbon atoms and an aryl group having 5 to 10 carbon atoms; and Ar is an aromatic nucleus, provided that either R.sup.2 or Ar contains fat least one electron withdrawing group in addition to the chlorine, said electron withdrawing group having a Hammett sigma constant with a value greater than 0.10 and excluding halogen,

2. The process of claim 1 wherein the iodide salt is present in an amount of 0.25 to 2.5 equivalents based on the equivalents of aromatic chloride, the transition metal catalyst is present in an amount of 0.01 to 0.1 equivalents based on the equivalents of aromatic chloride, the base is present in an amount of 0.5 to 10 equivalents based on the equivalents of aromatic chloride, and the organic solvent is present in an amount of 1 to 5000 weight percent based on the weight of aromatic chloride.

3. The process of claim 2 wherein the base is present in an amount of 1 to 5 equivalents based on the equivalents of aromatic chloride, and the organic solvent is present in an amount of 1000 to 5000 weight percent based on the weight of aromatic chloride.

4. The process of claim 1 wherein the electron withdrawing group is selected from the group consisting of sulfone, ketone, ester, phthalimido, and nitrile.

5. The process of claim 1 wherein the amine is a monoamine selected from the group consisting of methylamine, ethylamine, n-propylamine, isopropylamine, n-butylamine, n-octylamine, dodecylamine, cyclohexylamine, dimethylamine, diethylamine, diisopropylamine, dibutylamine, ethylisopropylamine, piperidine, morpholine, pyrrolidine, aniline, o-toluidine, m-toluidine, p-toluidine, m-methoxyaniline, p-methoxyaniline, p-dimethylaminoaniline, p-aminomethylbenzoate, p-aminobenzonitrile, p-aminoacetophenone, 1-aminonaphthalene, 2-aminonaphthalene, and combinations thereof.

6. The process of claim 1 wherein the amine is a polyfunctional amine selected from the group consisting of ##STR15## bis(3-aminopropyl)tetramethyldisiloxane for x=1, ##STR16## ethylenediamine, propylenediamine, piperazine, and combinations thereof.

7. The process of claim 6 wherein the amine is aniline.

8. The process of claim 1 wherein the aromatic chloride is a monoaromatic chloride selected from the group consisting of ##STR17## 4-chloronitrobenzene, and combinations thereof.

9. The process of claim 1 wherein the aromatic chloride is a polyaromatic chloride selected from the group consisting of 4,4'-dichlorodiphenylsulfone, 4,4'-dichlorobenzophenone, 4,4'-dichloro-9,10-anthraquinone, 2,6-dichloro-9,10-anthraquinone, 2,7-dichloro-9,10-anthraquinone, and compounds having the structure ##STR18##

1. 3,5-tris(4-chlorophenylsulfonyl)benzene and combinations thereof.

10. The process of claim 1 wherein the iodide salt is selected from the group consisting of sodium iodide, lithium iodide, potassium iodide, magnesium iodide, and calcium iodide or other dissociative iodide salts.

11. The process of claim 10 wherein the iodide salt is sodium iodide.

12. The process of claim 1 wherein the catalyst is selected from the group consisting of platinum, nickel, and palladium complexes.

13. The process of claim 12 wherein the palladium complex is a palladium salt having the formula PdX.sub.2 wherein X is Cl, Br or I.

14. The process of claim 13 wherein the palladium complex is bis(triphenylphosphene)palladium(II) chloride.

15. The process of claim 1 which additionally contains a ligand in an amount of 0.01 moles to 5 moles per mole of transition metal catalyst.

16. The process of claim 15 wherein said ligand is 1,2-diphenylphosphine ethane.

17. The process of claim 1 wherein the base is selected from the group consisting of tertiary amines, NR.sub.3 wherein R is independently selected from lower alkyl groups having 2 to 6 carbon atoms, and combinations thereof.

18. The process of claim 17 wherein the base is a tertiary amine selected from the group consisting of tributylamine, 1,3-diazobicyclo(5,4,0)-7-undecene, 1,5-diazobicyclo(4,3,0)non-5-ene, and combinations thereof.

19. The process of claim 1 which additionally contains an organic solvent in an amount of 0.1 to 10,000 weight percent based on the weight of aromatic chloride.

20. The process of claim 19 wherein the organic solvent is selected from the group consisting of hydrocarbon solvents having C.sub.5 -C.sub.20, ether solvents characterized by R'OR' wherein R' is an aliphatic or aromatic hydrocarbon having C.sub.4 -C.sub.10, and dipolar aprotic solvents.

21. The process of claim 20 wherein the organic solvent is a dipolar aprotic solvent.

22. The process of claim 21 wherein the dipolar aprotic solvent is selected from the group consisting of N,N-dimethylformamide, N,N-dimethylacetamide, dimethyl-sulfoxide, 1,3-dimethyl-2-imidazolidinone, hexamethylphosphoramide, N-methylpyrrolidinone, N-cyclohexylpyrrolidinone, dimethylimidazolidinone, and mixtures thereof.

23. The process of claim 22 wherein the dipolar aprotic solvent is N,N-dimethylacetamide.